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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22656생성일: 2026년 10월 23일

Acetic Anhydride → Methyl 1-acetyl-1H-indazole-5-carboxylate

https://huagongshe.com/ko/reaction/22656

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Pentyl nitriteHCID 10026—
반응물18-Crown-6HCID 28557—
반응물Potassium AcetateHCID 517044—
반응물Methyl 4-amino-3-methylbenzoateHCID 2736799—
용매ChloroformHCID 6212—
생성물Methyl 1-acetyl-1H-indazole-5-carboxylateHCID 2259133247.4%

반응 단계

To a stirred mixture of methyl 3-methyl-4-aminobenzoate (5.0 g, 30.0 mmol) and potassium acetate (2.94 g, 30.0 mmol) in chloroform (50 mL) is added acetic anhydride (5.66 mL, 60.0 mmol). The mixture is stirred for 30 min at rt, followed by the addition of 18-crown-6 (1.58 g, 6.0 mmol) and n-amyl nitrite (7.78 g, 66.0 mmol). The mixture is heated to reflux for 16 h, followed by cooling to rt. The mixture is washed sequentially with aqueous sodium bicarbonate solution (2×), water and brine. The organic layer is dried over MgSO4, filtered and concentrated in vacuo. The crude product is purified by flash chromatography on silica gel. Elution with hexanes-EtOAc (80:20) gives 3.1 g (47%) of methyl 1-acetyl-1H-indazole-5-carboxylate as a yellow solid: 1H NMR (400 MHz, CDCl3) δ 8.52-8.50, 8.3, 8.2, 4.0, 2.8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849620B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-6062662749034ec397236ef61309513e
출처 메모uspto-grants-2005_02